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EMG and NCV
Objective
To familiarize Nerve Conduction Studies & Needle Electromyography as
diagnostic tools and interpret its findings
EMG & NCV 2
Contents
1. Background
2. Basic Instrumentations
3. Sensory and Motor Nerve Conduction Studies
4. Late responses
5. Electromyography
6. Clinical Interpretations
EMG & NCV 3
Electrodiagnosis
• Electrodiagnosis is the field of study that uses electrical technology to
study human neurophysiology. (Adam et al, 2020)
Types
• Conventional Electrodiagnostic Test
• Modern Diagnostic Tests
EMG & NCV 4
Conventional Electrodiagnostic Test
Strength Duration Curve
EMG & NCV 5
Rheobase Test
Chronaxie Test
Faradic/Galvanic Test
Reaction of Degeneration Test
Pulse Ratio
Accommodation
Galvanic Tetanus Ratio
Modern Electrodiagnostic Test
Electromyography (EMG)
EMG & NCV 6
Nerve Conduction Velocity (NCV)
Late Response
Repetitive Nerve Stimulation
Evoked Potential Studies
Indication of EMG & NCV
1. Suspected Neuromuscular diseases
• Nerve root pathology
• Nerve/Plexus pathology
• Neuromuscular junction pathology
• Muscle pathology
2. Follow up
EMG & NCV 7
Jay M Weiss, Lyn D Weiss. Easy EMG. Boston (USA): Elsevier; 2016.
Instrumentations
EMG & NCV 8
Electrodes
EMG & NCV 9
Surface Electrodes
Disc Ring Ground
Electrodes
EMG & NCV 10
Stimulating Electrodes
Electrodes
EMG & NCV 11
Concentric Monopolar Bipolar Concentric
Needle Electrodes
Processing Unit
Amplifier
Filter
Signal Averager
Analog to Digital Conversion
EMG & NCV 12
Display System
1. Video Computer screen
2. Audio System
Sweep speed: Horizontal screen=
milliseconds
Sensitivity: vertical axis= response
amplitude
EMG & NCV 13
Nerve Condition Studies
Test used to measure the speed of the electrical activity of a nerve
Nerve conduction studies can test sensory or motor nerve fibers and can
determine both the speed of conduction as well as the amplitude of the
electrical signal evoked following stimulation of a nerve. (Julie K et al, 2016)
EMG & NCV 14
Nerve Condition Studies
Types
1. Sensory Nerve Condition Studies
2. Motor Nerve Conduction Studies
3. Late Responses- (F- wave & H- reflex)
4. Repetitive Nerve Stimulation
EMG & NCV 15
Nerve Condition Studies
Advantage
1. Differentiate Axonal loss from demyelination
2. Localizes the site of injury
3. Can assess severity of nerve lesion
4. Can distinguish the type of nerve lesion
5. Non invasive technique
EMG & NCV 16
Jay M Weiss, Lyn D Weiss. Easy EMG. Boston (USA): Elsevier; 2016.
Nerve Condition Studies
Limitations
1. Routine studies primarily evaluate distal nerves
2. Very Mild axon loss without demyelination may not be detected.
3. Some deeper nerve branches cannot be easily tested.
4. It does not evaluate small fibers
EMG & NCV 17
Jun Kimura. Electrodiagnosis in Nerve and Muscles fourth edition. Kyoto (JAP): oxford; 2012.
Nerve Condition Studies
Patient Preparation:
Informed Consent
Examine skin
Relaxed comfortable position
True Nerve length
Maintain skin temperature
Clean the skin with alcohol swab
EMG & NCV 18
Nerve Condition Studies
Stimulation:
EMG & NCV 19
Orthodromic Stimulation Antidromic Stimulation
Physiological direction
Nerve Condition Studies
Distance Measurement:
EMG & NCV 20
Sensory Nerve Condition Studies
Basic Principle of Nerve Stimulation
1. Sensory nerve is stimulated at one point where as Motor nerve is stimulated at
least 2 points along its course
2. Supramaximal stimulation is applied for Sensory Nerve Action Potential (SNAP)
and Compound Motor Action Potential (CMAP)
3. Cathode pole of electrode (Black) should be placed near to the active electrode
EMG & NCV 21
Jun Kimura. Electrodiagnosis in Nerve and Muscles fourth edition. Kyoto (JAP): oxford; 2012.
Sensory Nerve Condition Studies
Electrode Placement : Sensory NCV
EMG & NCV 22
Electrode Site
Active (Recording) Over the nerve
Reference 3-4 cm apart from
Active electrode
Stimulating
electrode
Along the course
of nerve to be
stimulated
Ground Between Active
and stimulating
Electrode
Motor Nerve Condition Studies
Electrode Placement: Motor NCV
EMG & NCV 23
Electrode Site
Active
(Recording)
Over the muscle belly (motor
point)
Reference (E2
or G2)
Nearby Tendon or bone away
from the muscle
Stimulating
electrode
Along the course of nerve to
be stimulated
Ground Between Active and
stimulating Electrode
Nerve Condition Studies
Sensory Nerve Action Potential (SNAP)
EMG & NCV 24
Compound Motor Action Potential (CMAP)
Nerve Condition Studies
1. Latency:
 Time taken electrical impulse to travel from the
stimulation site to the recording site
 Sensory Nerve: Depends upon the speed of
conduction of the fastest fiber and distance
between stimulus to active electrodes
 Motor Nerve: Depends upon the speed of
conduction of the fastest fiber , distance
between stimulus to active electrodes,
neuromuscular transmission time and
propagation time along the muscle membrane.
EMG & NCV 25
Nerve Condition Studies
2. Duration :
Measured from initial
negative peak to return to
baseline
Suggest the number of
nerve fiber
EMG & NCV 26
Nerve Condition Studies
3. Amplitude:
Measured from baseline to
negative peak or negative
peak to positive peak
Suggest the density of nerve
fiber in Sensory NCS and
number of motor units in
Motor NCS.
EMG & NCV 27
Nerve Condition Studies
4. Nerve Conduction Velocity (NCV):
EMG & NCV 28
Distance between Active and stimulating electrode
onset latency
SNCV =
Distance between proximal and distal Stimulating site
Proximal latency- distal latency
MNCV =
Normative value :Amplitude
EMG & NCV 29
Sensory
NCV
Nerve Amplitude
(micro Volt)
Nerve Amplitude
(micro Volt)
Median (S) >20.0 Sural (S) >10.0
Ulnar (S) >18.0 Lat Femoral
Cutaneous
10-25
Radial (S) >10.0 Superficial
fibular (S)
10-26
Motor NCV
Nerve Amplitude
(m Volt)
Nerve Amplitude
(m Volt)
Median (M) >4.0 Fibular >2.0
Ulnar (M) >4.0 Medial Plantar >3.0
Radial (M) >3.0 Lateral plantar >3.0
Normative Value :NCV
EMG & NCV 30
Sensory CV
Nerve Velocity (m/s) Nerve Velocity (m/s)
Median (S) >45.0 Sural (S) >36.0
Ulnar (S) >45.0 Lat Femoral
Cutaneous
> 44
Radial (S) >44.0 Superficial
fibular (S)
45.5-56.9
Motor CV
Nerve Velocity (m/s) Nerve Velocity (m/s)
Median (M) >50.0 Fibular >40.0
Ulnar (M) >50.0 Medial Plantar > 40.0
Radial (M) >50.0 Lateral plantar >40.0
Normative Value :Distal Latency
EMG & NCV 31
Sensory CV
Nerve Latency (ms) Nerve Latency (ms)
Median (S) <1.9 Sural (S) <3.8
Ulnar (S) <3.1 Lat Femoral
Cutaneous
<2.6
Radial (S) <3.4 Superficial
fibular (S)
<2.4
Motor CV
Nerve Velocity (m/s) Nerve Velocity (m/s)
Median (M) <4.2 Fibular <5.5
Ulnar (M) <3.4 Medial Plantar <6.0
Radial (M) <2.9 Lateral plantar <6.0
To Memorize
EMG & NCV 32
Nerve Upper limb Lower Limb
Latency <4.0 ms <6.0 ms
Sensory Amplitude >10.0 µV >10.0 µV
Motor Amplitude >4.0 mV >3.0 mV
NCV 40-50 m/s 35-45 m/s
H Reflex
EMG & NCV 33
 Monosynaptic reflex
 Assess proximal lesions
 Submaximal stimulation
 Involves sensory and motor neurons
 Reflex arch of H Reflex:
• Ia sensory fiber
• Spinal cord and its interneuron
• Efferent motor fiber
Supramaximal stimulation: No H-
reflex
H Reflex
EMG & NCV 34
Normal value in Soleus H
reflex in adults
• Latency (ms): 30.3 ± 1.7
• Amplitude (mV): 9.8 ± 6.1
• M-wave (mV): 24.6 ±6.6
• HM ratio: 0.4 ± 0.2
Clinical Implications
• Evaluates proximal sensory & motor
pathways
• GBS: absent, delayed or dispersed
• S1 radiculopathy: delayed or absent
F Wave
EMG & NCV 35
 Supramaximal stimulation
 No reflex arch
 Evaluates
 Root or plexus abnormalities
 Neuropathy
 myopathy
 Helpful in diagnosis of
 GBS
 Thoracic outlet syndrome
 Brachial plexus injury
 Radiculopathies with more than
one root involved
F Wave
EMG & NCV 36
Properties
1. Latency (ms): 16.3 ± 1.9
2. Amplitude(mV): 0.2 ± 0.1
3. Duration (ms): 7.6 ± 1.4
4. F –M ratio: 0.8-0.2
5. Chronodispersion: 2.5 ±1.1
Interpretation of NCV Studies
EMG & NCV 37
Normal
Axonal Degeneration
Demyelinating
Wrist
Elbow
Gullian Barre Syndrome
EMG & NCV 38
INCREASED
REDUCTION
PROXIMAL LATENCY
CMAP
AMPLITUDE
Diabetic neuropathy
EMG & NCV 39
DISTAL LATENCY
CMAP AMPLITUDE
SNAP AMPLITUDE
NORMAL OR
NEAR NORMAL
REDUCTION
REDUCTION
Radiculopathy
EMG & NCV 40
CMAP AMPLITUDE
F WAVE
H REFLEX REDUCED/ABSENT
REDUCTION
REDUCED/ABSENT
Pronater teres syndrome
EMG & NCV 41
PROXIMAL LATENCY AT
FOREARM
DISTAL LATENCY AT
WRIST
CMAP AMPLITUDE
FOREARM
WRIST
PROLONGED
NORMAL
NORMAL
Variables affecting NCV Studies
EMG & NCV 42
Physiological Variables Technical variables
Age Stimulating system
Temperature Recording System
Upper limb vs Lower limb Inadvertent stimulation of
another nerve
Gender Anomalous innervation of
muscles
Electromyography (EMG)
• Recording of action potential of muscle fibers firing singly or in a group, near the
needle electrode in a muscles (Mishra & Kalita, 2014)
• EMG test the integrity of entire motor system, which consists of upper and lower
motor neurons, neuromuscular junction and muscles (Kimura, 2016)
• Performed as an extension of physical examination rather than laboratory
procedure.
EMG & NCV 43
Electromyography (EMG)
EMG & NCV 44
NEEDLE EMG
SURFACE EMG
Special Precautions for EMG
• Morbid Obesity
• Thin Individuals
• Bleeding disorders
• Aseptic precaution
EMG & NCV 45
Contraindication for EMG
• Recent systemic infectious diseases
• Recent muscle biopsy
• Localized inflammation
• Skin lesions
EMG & NCV 46
EMG Procedure
• Preparation of patient
• Select the muscles to be tested
• Locate the site of needle insertion
• Insert the needle quickly
• Sharp Motor Unit Potential (MUP) on minimal voluntary contraction
confirms that needle is in proper position. If MUP is not sharp,
reposition the needle
EMG & NCV 47
Neuropathy vs Myopathy
EMG & NCV 48
Neuropathy Myopathy
Number of motor neuron decreases Muscle fibers are destroyed
Deprived muscles fibers get collateral from
viable motor neuron
Decreased number of muscle fibers
supplied by a single motor neuron
Increased number of muscle fibers supplied
by a single motor neuron
Decrease in size of motor unit
Amplitude and duration of Motor unit action
potential increases
Amplitude and duration of Motor unit
action potential decreases
EMG Analysis
1. Insertional Activity
2. Muscles at Rest
3. Motor Unit Analysis on mild voluntary contraction
4. Maximum voluntary contraction
• Recruitment pattern
• Interference pattern
EMG & NCV 49
Insertional activity
EMG & NCV 50
Insertional activity
EMG & NCV 51
Insertional activity
Insertional activity Seen in
Increased Early stage of denervation
Acute myositis
Inflammatory myopathies
Decreased Atrophied muscles
Fibrosed muscles
Needle electrode is not in
muscle tissue
EMG & NCV 52
Examination of Muscles at Rest
1.No activity
2. Endplate region:
1. Miniature Endplate
Potentials (MEEP)
2. Endplate spike
3. Spontaneous Activity
EMG & NCV 53
Examination of Muscles at Rest
Endplate region:
EMG & NCV 54
Spontaneous Activity
Originated from Muscle Fibers Originated from motor neuron
1.Fibrillation Potentials (Fibs)
2.Positive sharp waves (PSW)
3.Myotonic Discharge
4.Complex repetitive discharges
1.Myokymic discharge
2.Cramps
3.Neuromyotonic discharge
4.Fasciculation
5.Fibrillation Potentials (Fibs)
EMG & NCV 55
Spontaneous activities
1. Positive Sharp Wave
EMG & NCV 56
Seen in:
1. Mainly on Lower Motor
Neuron Lesion
2. Also seen in Myopathies
Spontaneous activities
EMG & NCV 57
2. Fibrillation Potential Seen in
1. LMNL
2. Myopathies
Spontaneous activities
Positive Sharp Wave and Fibrillation Potential
EMG & NCV 58
Spontaneous Activity
3. Complex Repetitive Discharge (CRD)
EMG & NCV 59
Seen in
Myogenic conditions
Polymyositis
Muscular dystrophies
Neurogenic Conditions
Poliomyelitis
ALS
Chronic radiculopathies
Chronic neuropathies
Spontaneous Activity
3. Complex Repetitive Discharge (CRD)
EMG & NCV 60
Abnormal Spontaneous Activity
Seen in
Myotonic dystrophy
Polymyositis
Chronic radiculopathy
EMG & NCV 61
4. Myotonic discharge
Abnormal Spontaneous Activity
EMG & NCV 62
4. Myotonic discharge
Abnormal Spontaneous Activity
5. Myokymic discharge
EMG & NCV 63
Seen in
Facial Muscles:
Bells palsy
Multiple sclerosis
Polyradiculopathy
Limb muscles
Chronic nerve lesions
Abnormal Spontaneous Activity
5. Myokymic discharge
EMG & NCV 64
Abnormal Spontaneous Activity
6. Fasciculation
EMG & NCV 65
Seen in
Small twitch
Irritation of AHC
Chronic peripheral nerve lesions
Nerve root compression
Muscle spasm or cramps
ALS and PMA (motor neuron
diseases)
Abnormal Spontaneous Activity
6. Fasciculation
EMG & NCV 66
Motor Unit Action Potential (MUAP)
• Analysis of MUAP done with
minimal contraction of muscles
EMG & NCV 67
Motor Unit Action Potential (MUAP)
Component Normative value
Amplitude 4 µV to 5 mV
Duration 2 ms to 17 ms
Rise time Upto 500 ms
Frequency 1 Hz- 60 Hz
Phase Mono to Four
phases
(Bi-phasic or Tri-
phasic)
Sound Clear, sharp
EMG & NCV 68
Motor Unit Action Potential (MUAP)
EMG & NCV 69
Motor Unit Action Potential (MUAP)
EMG & NCV 70
Amplitude and Duration
Increased in Neuropathy
Decreased in myopathy
Motor Unit Action Potential (MUAP)
EMG & NCV 71
Phases
Normal triphasic
Polyphasic
+ Longer
Duration
Neurogenic abnormalities
+ Shorter Myopathic
Examination of Muscles at Maximum
Voluntary Contraction
• Change in electrical activity during progressively increasing
contraction to maximal contraction
1. Recruitment
2. Interference pattern
EMG & NCV 72
Recruitment & Interference
• The motor unit start firing in a regular pattern at 5 Hz
EMG & NCV 73
Normal
Neurogenic
Myopathic
Normal Interference Pattern
EMG & NCV 74
Myopathy Interference Pattern
EMG & NCV 75
Neurogenic Interference Pattern
EMG & NCV 76
EMG finding in DMD
EMG & NCV 77
DECREASED/ ABSENT
Fibrillation Potential, Positive sharp waves
Low amplitude, Short duration, Polyphasic
Low amplitude and Reduced
Insertional Activity
Spontaneous
Activity
Motor Unit Potential
Interference
EMG finding in Gullian Barre Syndrome
EMG & NCV 78
Increased
Fasciculation or Myokymic
High amplitude, long duration, Polyphasic
High amplitude and Reduced
Insertional Activity
Spontaneous
Activity
Motor Unit Potential
Interference
Role of EMG and NCV Tests in Physiotherapy
EMG & NCV 79
EVALUATE TREATMENT OUTCOME
NEUROMUSCULOSKELETAL ASSESSMENT
PLAN PHYSIOTHERAPY INTERVENTION
Take Home Message
1. NCV : demyelinating and axonal neuropathy
2. Late responses (F wave and H-reflex) : Radiculopathy and proximal neuropathy
3. Electromyography studies differentiates myopathy with neuropathy
4. All these tests are extensions of physical examinations
5. Findings of Electrodiagnosis tests can be valuable to plan physiotherapy
interventions based on severity and type of neuromusculoskeletal injuries
EMG & NCV 80
THANK YOU
EMG & NCV 81

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NCV and EMG.pptx

  • 2. Objective To familiarize Nerve Conduction Studies & Needle Electromyography as diagnostic tools and interpret its findings EMG & NCV 2
  • 3. Contents 1. Background 2. Basic Instrumentations 3. Sensory and Motor Nerve Conduction Studies 4. Late responses 5. Electromyography 6. Clinical Interpretations EMG & NCV 3
  • 4. Electrodiagnosis • Electrodiagnosis is the field of study that uses electrical technology to study human neurophysiology. (Adam et al, 2020) Types • Conventional Electrodiagnostic Test • Modern Diagnostic Tests EMG & NCV 4
  • 5. Conventional Electrodiagnostic Test Strength Duration Curve EMG & NCV 5 Rheobase Test Chronaxie Test Faradic/Galvanic Test Reaction of Degeneration Test Pulse Ratio Accommodation Galvanic Tetanus Ratio
  • 6. Modern Electrodiagnostic Test Electromyography (EMG) EMG & NCV 6 Nerve Conduction Velocity (NCV) Late Response Repetitive Nerve Stimulation Evoked Potential Studies
  • 7. Indication of EMG & NCV 1. Suspected Neuromuscular diseases • Nerve root pathology • Nerve/Plexus pathology • Neuromuscular junction pathology • Muscle pathology 2. Follow up EMG & NCV 7 Jay M Weiss, Lyn D Weiss. Easy EMG. Boston (USA): Elsevier; 2016.
  • 9. Electrodes EMG & NCV 9 Surface Electrodes Disc Ring Ground
  • 10. Electrodes EMG & NCV 10 Stimulating Electrodes
  • 11. Electrodes EMG & NCV 11 Concentric Monopolar Bipolar Concentric Needle Electrodes
  • 13. Display System 1. Video Computer screen 2. Audio System Sweep speed: Horizontal screen= milliseconds Sensitivity: vertical axis= response amplitude EMG & NCV 13
  • 14. Nerve Condition Studies Test used to measure the speed of the electrical activity of a nerve Nerve conduction studies can test sensory or motor nerve fibers and can determine both the speed of conduction as well as the amplitude of the electrical signal evoked following stimulation of a nerve. (Julie K et al, 2016) EMG & NCV 14
  • 15. Nerve Condition Studies Types 1. Sensory Nerve Condition Studies 2. Motor Nerve Conduction Studies 3. Late Responses- (F- wave & H- reflex) 4. Repetitive Nerve Stimulation EMG & NCV 15
  • 16. Nerve Condition Studies Advantage 1. Differentiate Axonal loss from demyelination 2. Localizes the site of injury 3. Can assess severity of nerve lesion 4. Can distinguish the type of nerve lesion 5. Non invasive technique EMG & NCV 16 Jay M Weiss, Lyn D Weiss. Easy EMG. Boston (USA): Elsevier; 2016.
  • 17. Nerve Condition Studies Limitations 1. Routine studies primarily evaluate distal nerves 2. Very Mild axon loss without demyelination may not be detected. 3. Some deeper nerve branches cannot be easily tested. 4. It does not evaluate small fibers EMG & NCV 17 Jun Kimura. Electrodiagnosis in Nerve and Muscles fourth edition. Kyoto (JAP): oxford; 2012.
  • 18. Nerve Condition Studies Patient Preparation: Informed Consent Examine skin Relaxed comfortable position True Nerve length Maintain skin temperature Clean the skin with alcohol swab EMG & NCV 18
  • 19. Nerve Condition Studies Stimulation: EMG & NCV 19 Orthodromic Stimulation Antidromic Stimulation Physiological direction
  • 20. Nerve Condition Studies Distance Measurement: EMG & NCV 20
  • 21. Sensory Nerve Condition Studies Basic Principle of Nerve Stimulation 1. Sensory nerve is stimulated at one point where as Motor nerve is stimulated at least 2 points along its course 2. Supramaximal stimulation is applied for Sensory Nerve Action Potential (SNAP) and Compound Motor Action Potential (CMAP) 3. Cathode pole of electrode (Black) should be placed near to the active electrode EMG & NCV 21 Jun Kimura. Electrodiagnosis in Nerve and Muscles fourth edition. Kyoto (JAP): oxford; 2012.
  • 22. Sensory Nerve Condition Studies Electrode Placement : Sensory NCV EMG & NCV 22 Electrode Site Active (Recording) Over the nerve Reference 3-4 cm apart from Active electrode Stimulating electrode Along the course of nerve to be stimulated Ground Between Active and stimulating Electrode
  • 23. Motor Nerve Condition Studies Electrode Placement: Motor NCV EMG & NCV 23 Electrode Site Active (Recording) Over the muscle belly (motor point) Reference (E2 or G2) Nearby Tendon or bone away from the muscle Stimulating electrode Along the course of nerve to be stimulated Ground Between Active and stimulating Electrode
  • 24. Nerve Condition Studies Sensory Nerve Action Potential (SNAP) EMG & NCV 24 Compound Motor Action Potential (CMAP)
  • 25. Nerve Condition Studies 1. Latency:  Time taken electrical impulse to travel from the stimulation site to the recording site  Sensory Nerve: Depends upon the speed of conduction of the fastest fiber and distance between stimulus to active electrodes  Motor Nerve: Depends upon the speed of conduction of the fastest fiber , distance between stimulus to active electrodes, neuromuscular transmission time and propagation time along the muscle membrane. EMG & NCV 25
  • 26. Nerve Condition Studies 2. Duration : Measured from initial negative peak to return to baseline Suggest the number of nerve fiber EMG & NCV 26
  • 27. Nerve Condition Studies 3. Amplitude: Measured from baseline to negative peak or negative peak to positive peak Suggest the density of nerve fiber in Sensory NCS and number of motor units in Motor NCS. EMG & NCV 27
  • 28. Nerve Condition Studies 4. Nerve Conduction Velocity (NCV): EMG & NCV 28 Distance between Active and stimulating electrode onset latency SNCV = Distance between proximal and distal Stimulating site Proximal latency- distal latency MNCV =
  • 29. Normative value :Amplitude EMG & NCV 29 Sensory NCV Nerve Amplitude (micro Volt) Nerve Amplitude (micro Volt) Median (S) >20.0 Sural (S) >10.0 Ulnar (S) >18.0 Lat Femoral Cutaneous 10-25 Radial (S) >10.0 Superficial fibular (S) 10-26 Motor NCV Nerve Amplitude (m Volt) Nerve Amplitude (m Volt) Median (M) >4.0 Fibular >2.0 Ulnar (M) >4.0 Medial Plantar >3.0 Radial (M) >3.0 Lateral plantar >3.0
  • 30. Normative Value :NCV EMG & NCV 30 Sensory CV Nerve Velocity (m/s) Nerve Velocity (m/s) Median (S) >45.0 Sural (S) >36.0 Ulnar (S) >45.0 Lat Femoral Cutaneous > 44 Radial (S) >44.0 Superficial fibular (S) 45.5-56.9 Motor CV Nerve Velocity (m/s) Nerve Velocity (m/s) Median (M) >50.0 Fibular >40.0 Ulnar (M) >50.0 Medial Plantar > 40.0 Radial (M) >50.0 Lateral plantar >40.0
  • 31. Normative Value :Distal Latency EMG & NCV 31 Sensory CV Nerve Latency (ms) Nerve Latency (ms) Median (S) <1.9 Sural (S) <3.8 Ulnar (S) <3.1 Lat Femoral Cutaneous <2.6 Radial (S) <3.4 Superficial fibular (S) <2.4 Motor CV Nerve Velocity (m/s) Nerve Velocity (m/s) Median (M) <4.2 Fibular <5.5 Ulnar (M) <3.4 Medial Plantar <6.0 Radial (M) <2.9 Lateral plantar <6.0
  • 32. To Memorize EMG & NCV 32 Nerve Upper limb Lower Limb Latency <4.0 ms <6.0 ms Sensory Amplitude >10.0 µV >10.0 µV Motor Amplitude >4.0 mV >3.0 mV NCV 40-50 m/s 35-45 m/s
  • 33. H Reflex EMG & NCV 33  Monosynaptic reflex  Assess proximal lesions  Submaximal stimulation  Involves sensory and motor neurons  Reflex arch of H Reflex: • Ia sensory fiber • Spinal cord and its interneuron • Efferent motor fiber Supramaximal stimulation: No H- reflex
  • 34. H Reflex EMG & NCV 34 Normal value in Soleus H reflex in adults • Latency (ms): 30.3 ± 1.7 • Amplitude (mV): 9.8 ± 6.1 • M-wave (mV): 24.6 ±6.6 • HM ratio: 0.4 ± 0.2 Clinical Implications • Evaluates proximal sensory & motor pathways • GBS: absent, delayed or dispersed • S1 radiculopathy: delayed or absent
  • 35. F Wave EMG & NCV 35  Supramaximal stimulation  No reflex arch  Evaluates  Root or plexus abnormalities  Neuropathy  myopathy  Helpful in diagnosis of  GBS  Thoracic outlet syndrome  Brachial plexus injury  Radiculopathies with more than one root involved
  • 36. F Wave EMG & NCV 36 Properties 1. Latency (ms): 16.3 ± 1.9 2. Amplitude(mV): 0.2 ± 0.1 3. Duration (ms): 7.6 ± 1.4 4. F –M ratio: 0.8-0.2 5. Chronodispersion: 2.5 ±1.1
  • 37. Interpretation of NCV Studies EMG & NCV 37 Normal Axonal Degeneration Demyelinating Wrist Elbow
  • 38. Gullian Barre Syndrome EMG & NCV 38 INCREASED REDUCTION PROXIMAL LATENCY CMAP AMPLITUDE
  • 39. Diabetic neuropathy EMG & NCV 39 DISTAL LATENCY CMAP AMPLITUDE SNAP AMPLITUDE NORMAL OR NEAR NORMAL REDUCTION REDUCTION
  • 40. Radiculopathy EMG & NCV 40 CMAP AMPLITUDE F WAVE H REFLEX REDUCED/ABSENT REDUCTION REDUCED/ABSENT
  • 41. Pronater teres syndrome EMG & NCV 41 PROXIMAL LATENCY AT FOREARM DISTAL LATENCY AT WRIST CMAP AMPLITUDE FOREARM WRIST PROLONGED NORMAL NORMAL
  • 42. Variables affecting NCV Studies EMG & NCV 42 Physiological Variables Technical variables Age Stimulating system Temperature Recording System Upper limb vs Lower limb Inadvertent stimulation of another nerve Gender Anomalous innervation of muscles
  • 43. Electromyography (EMG) • Recording of action potential of muscle fibers firing singly or in a group, near the needle electrode in a muscles (Mishra & Kalita, 2014) • EMG test the integrity of entire motor system, which consists of upper and lower motor neurons, neuromuscular junction and muscles (Kimura, 2016) • Performed as an extension of physical examination rather than laboratory procedure. EMG & NCV 43
  • 44. Electromyography (EMG) EMG & NCV 44 NEEDLE EMG SURFACE EMG
  • 45. Special Precautions for EMG • Morbid Obesity • Thin Individuals • Bleeding disorders • Aseptic precaution EMG & NCV 45
  • 46. Contraindication for EMG • Recent systemic infectious diseases • Recent muscle biopsy • Localized inflammation • Skin lesions EMG & NCV 46
  • 47. EMG Procedure • Preparation of patient • Select the muscles to be tested • Locate the site of needle insertion • Insert the needle quickly • Sharp Motor Unit Potential (MUP) on minimal voluntary contraction confirms that needle is in proper position. If MUP is not sharp, reposition the needle EMG & NCV 47
  • 48. Neuropathy vs Myopathy EMG & NCV 48 Neuropathy Myopathy Number of motor neuron decreases Muscle fibers are destroyed Deprived muscles fibers get collateral from viable motor neuron Decreased number of muscle fibers supplied by a single motor neuron Increased number of muscle fibers supplied by a single motor neuron Decrease in size of motor unit Amplitude and duration of Motor unit action potential increases Amplitude and duration of Motor unit action potential decreases
  • 49. EMG Analysis 1. Insertional Activity 2. Muscles at Rest 3. Motor Unit Analysis on mild voluntary contraction 4. Maximum voluntary contraction • Recruitment pattern • Interference pattern EMG & NCV 49
  • 52. Insertional activity Insertional activity Seen in Increased Early stage of denervation Acute myositis Inflammatory myopathies Decreased Atrophied muscles Fibrosed muscles Needle electrode is not in muscle tissue EMG & NCV 52
  • 53. Examination of Muscles at Rest 1.No activity 2. Endplate region: 1. Miniature Endplate Potentials (MEEP) 2. Endplate spike 3. Spontaneous Activity EMG & NCV 53
  • 54. Examination of Muscles at Rest Endplate region: EMG & NCV 54
  • 55. Spontaneous Activity Originated from Muscle Fibers Originated from motor neuron 1.Fibrillation Potentials (Fibs) 2.Positive sharp waves (PSW) 3.Myotonic Discharge 4.Complex repetitive discharges 1.Myokymic discharge 2.Cramps 3.Neuromyotonic discharge 4.Fasciculation 5.Fibrillation Potentials (Fibs) EMG & NCV 55
  • 56. Spontaneous activities 1. Positive Sharp Wave EMG & NCV 56 Seen in: 1. Mainly on Lower Motor Neuron Lesion 2. Also seen in Myopathies
  • 57. Spontaneous activities EMG & NCV 57 2. Fibrillation Potential Seen in 1. LMNL 2. Myopathies
  • 58. Spontaneous activities Positive Sharp Wave and Fibrillation Potential EMG & NCV 58
  • 59. Spontaneous Activity 3. Complex Repetitive Discharge (CRD) EMG & NCV 59 Seen in Myogenic conditions Polymyositis Muscular dystrophies Neurogenic Conditions Poliomyelitis ALS Chronic radiculopathies Chronic neuropathies
  • 60. Spontaneous Activity 3. Complex Repetitive Discharge (CRD) EMG & NCV 60
  • 61. Abnormal Spontaneous Activity Seen in Myotonic dystrophy Polymyositis Chronic radiculopathy EMG & NCV 61 4. Myotonic discharge
  • 62. Abnormal Spontaneous Activity EMG & NCV 62 4. Myotonic discharge
  • 63. Abnormal Spontaneous Activity 5. Myokymic discharge EMG & NCV 63 Seen in Facial Muscles: Bells palsy Multiple sclerosis Polyradiculopathy Limb muscles Chronic nerve lesions
  • 64. Abnormal Spontaneous Activity 5. Myokymic discharge EMG & NCV 64
  • 65. Abnormal Spontaneous Activity 6. Fasciculation EMG & NCV 65 Seen in Small twitch Irritation of AHC Chronic peripheral nerve lesions Nerve root compression Muscle spasm or cramps ALS and PMA (motor neuron diseases)
  • 66. Abnormal Spontaneous Activity 6. Fasciculation EMG & NCV 66
  • 67. Motor Unit Action Potential (MUAP) • Analysis of MUAP done with minimal contraction of muscles EMG & NCV 67
  • 68. Motor Unit Action Potential (MUAP) Component Normative value Amplitude 4 µV to 5 mV Duration 2 ms to 17 ms Rise time Upto 500 ms Frequency 1 Hz- 60 Hz Phase Mono to Four phases (Bi-phasic or Tri- phasic) Sound Clear, sharp EMG & NCV 68
  • 69. Motor Unit Action Potential (MUAP) EMG & NCV 69
  • 70. Motor Unit Action Potential (MUAP) EMG & NCV 70 Amplitude and Duration Increased in Neuropathy Decreased in myopathy
  • 71. Motor Unit Action Potential (MUAP) EMG & NCV 71 Phases Normal triphasic Polyphasic + Longer Duration Neurogenic abnormalities + Shorter Myopathic
  • 72. Examination of Muscles at Maximum Voluntary Contraction • Change in electrical activity during progressively increasing contraction to maximal contraction 1. Recruitment 2. Interference pattern EMG & NCV 72
  • 73. Recruitment & Interference • The motor unit start firing in a regular pattern at 5 Hz EMG & NCV 73 Normal Neurogenic Myopathic
  • 77. EMG finding in DMD EMG & NCV 77 DECREASED/ ABSENT Fibrillation Potential, Positive sharp waves Low amplitude, Short duration, Polyphasic Low amplitude and Reduced Insertional Activity Spontaneous Activity Motor Unit Potential Interference
  • 78. EMG finding in Gullian Barre Syndrome EMG & NCV 78 Increased Fasciculation or Myokymic High amplitude, long duration, Polyphasic High amplitude and Reduced Insertional Activity Spontaneous Activity Motor Unit Potential Interference
  • 79. Role of EMG and NCV Tests in Physiotherapy EMG & NCV 79 EVALUATE TREATMENT OUTCOME NEUROMUSCULOSKELETAL ASSESSMENT PLAN PHYSIOTHERAPY INTERVENTION
  • 80. Take Home Message 1. NCV : demyelinating and axonal neuropathy 2. Late responses (F wave and H-reflex) : Radiculopathy and proximal neuropathy 3. Electromyography studies differentiates myopathy with neuropathy 4. All these tests are extensions of physical examinations 5. Findings of Electrodiagnosis tests can be valuable to plan physiotherapy interventions based on severity and type of neuromusculoskeletal injuries EMG & NCV 80
  • 81. THANK YOU EMG & NCV 81

Editor's Notes

  1. Has two Electrodes: Cathode/ Negative pole/Black Anode/Positive/ Red Cathode is placed towards the direction of stimulation (except F wave) Supramaximal stimulation: 10-12% Constant Current Stimulator and Constant Voltage Stimulator
  2. Severity of lesion: neuropraxia, Axonotmesis and Neurotmesis type of nerve lesion : sensory, motor or mixed
  3. 4: only fast fibers, myelinated fibers
  4. Examine skin: for sensitivity and integrity True Nerve length: For Ulnar nerve, flexed elbow Maintain skin temperature: at 34 degree Celsius.
  5. Motor NCV :The distance between two points should be at least 10 cm Normal Supramaximal stimulation for MNCV: 20-50 mA, SNCV: 5-30 mA Motor nerve is stimulated at least 2 points along its course : NMJ and muscle depolarizn time Cathode pole of stimulating electrode should be placed close to the active electrode : prevents hyperpolarization effect of anode and anodal conduction block
  6. CMAP: summative AP of motor units, more amplitude (mV), longer duration SNAP: summative AP of sensory N fibers, less amplitude (µV), shorter duration
  7. Skin Temp : 32 degree Celsius UE, 30 degree for LE Side to side amplitude difference of >50 % or 20 % amplitude drop distal to proximal is significant
  8. Skin Temp : 32 degree Celsius UE, 30 degree for LE Side to side amplitude difference of >50 % or 20 % amplitude drop distal to proximal is significant
  9. Skin Temp : 32 degree Celsius UE, 30 degree for LE Side to side amplitude difference of >50 % or 20 % amplitude drop distal to proximal is significant
  10. Skin Temp : 32 degree Celsius UE, 30 degree for LE, 8 cm distal stim site Side to side amplitude difference of >50 % or 20 % amplitude drop distal to proximal is significant
  11. Skin Temp : 32 degree Celsius UE, 30 degree for LE, distal latency 8 CM Side to side amplitude difference of >50 % or 20 % amplitude drop distal to proximal is significant
  12. Electrodes: Active: Gastrosoleus, Reference: TA, Stimulating: Popliteal fossa (for S1 radiculopathy) H reflex UE: Flexor carpi radialis, Median nerve at cubital fossa (C6-C7) radiculopathy H reflex disappear when stimulation is further increased Significance: Assess proximal lessions, becomes abnormal early in radiculopathy, assess preganglionic lesion Before 2 years Seen in every muscles Shorter conduction time of S1 due to less dispersion of Ia fiber of nerve
  13. Obtained from any distal muscles Depolarization of axon hillock—depolarization of dendrite—in turn depolarization of axon hillock select portion of these alpha motor neurons, (roughly 5-10% of available motor neurons), 'backfire' or rebound Only few (10%) of motor neuron particpitaes in F wave Explores only the motor component of peripheral nerve Small amplitude response occurring 20-60 ms after direct muscle response (m-wave)
  14. Chronodispersion: diff bw minimum and max latencies in series (50-60) of F wave F-M ratio: latencies of F wave: M wave Persistence: no of response occurrence divided by no of stimuli
  15. 50-75 % decrease in CMAP amplitude: moderate axon loss 75%: severe axonal loss Absent CMAP: no viable axon
  16. Primarily Demyelinating Neuropathy Proximal weakness Mainly affecting motor nerves
  17. Mainly axonal degeneration, distally
  18. Neuropraxia Compression of Median nerve at pronater teres, without conduction block
  19. Age: Infant has half NCV than adult: immature myelin sheet After 60 yrs NCV decreases: degeneration of nerve Temperature: Decrease in temp=latency increases, NCV decreases and amplitude increases Due to closure of ca channel 1 degree fall in temp incrases 0.3 ms latency Increasing temp (29-38), NCV increases by 5 % Idol skin temp : 34 degree Upper limb Vs lower limb Shorter UL nerve has longer internodal distance, large diameter of axon= increases NCV Longer LL nerve have many branches and lower temp than UL Male NCV<Female NCV (Fat increases core temp in female)
  20. Surface EMG assesses muscle function by recording muscle activity from the surface above the muscle on the skin. Surface EMG can be recorded by multiple electrodes. Limitations: Recordings are restricted to superficial muscles Uses: Kinesological Assessments, Research purpose and Biofeedback.
  21. Morbid obesity: difficult to localize specific muscles Thin individuals: not to insert needle deep to avoid injury to other tissues ( thoracis-lung)
  22. Needle location: slightly away from motor point to avoid end plate noise
  23. Insertional activity: caused by mechanical damage to muscles Spontaneou activity: muscles at rest
  24. Short burst of electrical activity (clusters of sharp positive and negative spike) lasts for < 300ms Insertional activity: caused by mechanical damage to muscles causing depolarization Sound: Crisp (wringing the paper)
  25. Increased: electrical activity lasts longer than 300 ms, due to unstable or excitable muscle fiber membrane Decreased: shorter
  26. Inflammatory myopathies Polymyositis, dermatomyositis Fibrosed muscles: muscular dystrophy diseases ( due to unsynhronous opening and closing of na-K channel) Denervation: acetylcholineesterage inhibition
  27. Miniature Endplate Potential (MEEP): spont release of ach , creates a small current short duration, irregular, small amplitude (10-20 microvolt) Endplate spike: large amount of ach release, produces short depolarizn single muscle fiber depolarization, biphasic, initial negative defletion, 100-200 microvolt, 3-5 msec Pain
  28. Endplate region: activity seen when the needle is in endplate region of a muscle fiber Miniature Endplate Potential (MEEP): spont release of ach , creates a small current short duration (1-2 ms), irregular, small amplitude (10-20 microvolt) Endplate spike: large amount of ach release, produces short depolarizn single muscle fiber depolarization, biphasic, initial negative defletion, 100-200 microvolt, 3-5 msec Pain
  29. PSW: small amplitude (20-100 µV) Mono or biphasic(primary +ve defln) , 0.5-15 Hz Arises from spont depolarization of a single muscle fiber Sound: dull thud; Appears earlier than Fibs after injury LMNL: AHC ds, Radiculopathies, PNI, Polyneuropathies with axonal degeneration Myopathies: Muscular dystrophies, polymyositis
  30. Fibs: rate: small amplitude 10-300µV; biphasic (initial positive) @ 05-10 hz, Arises from spont depolarization of a single muscle fiber Sound: rain hitting a tin roof LMNL: AHC ds, Radiculopathies, PNI, Polyneuropathies with axonal degeneration Myopathies: Muscular dystrophies, polymyositis
  31. PSW: dull thud; Appears earlier than Fibs after injury FIBS: rain hitting roofs
  32. CRD: local muscle arrhythmias, repetitive and regular firing of group of muscle fibers appear and disappear suddenly Suggests ongoing reinnervation originated by the spont depolarization of a single fiber, followed by ephaptic spread (cell to cell)to an adjacent muscle fiber. Frequency: 10-100 Hz, Amplitude: 50 microvolt-500 microvolt Sound: motorboat Usually seen in injury greater than 6 months (chronic neurogenic conditions and myopathies
  33. CRD: local muscle arrhythmias, repetitive and regular firing of group of muscle fibers Simple or complex spike pattern that appear suddenly and disappear Suggests ongoing reinnervation originated by the spont depolarization of a single fiber, followed by ephaptic spread (cell to cell)to an adjacent muscle fiber. Frequency: 10-100 Hz, Amplitude: 50 microvolt-500 microvolt Sound: motorboat Usually seen in injury greater than 6 months (chronic neurogenic conditions and myopathies
  34. myotonic:, waxing and waning appearance @ 20-100 hz rate: 20-100 hz Two forms of waves: psw morphology or Brief spikes pattern of biphasic or triphasic potentials originated by the spont depolarization of a single fiber, followed by ephaptic spread (cell to cell)to an adjacent muscle fiber. Sound: dive bomber Seen in myotonic dystrophy, polymyositis, chronic radiculopathy
  35. myotonic: rate: 20-100 hz, waxing and waning appearance Two forms of waves: psw morphology or Brief spikes pattern of biphasic or triphasic potentials originated by the spont depolarization of a single fiber, followed by ephaptic spread (cell to cell)to an adjacent muscle fiber. Sound: dive bomber (military aircraft) Seen in myotonic dystrophy, polymyositis, chronic radiculopathy
  36. Regular firing pattern and rhythms: 5-10 Hz Due to hyperexcitability of peripheral nerve motor axons Sound: soldier marching
  37. Regular firing pattern and rhythms: 5-10 Hz Due to hyperexcitability of peripheral nerve motor axons Sound: soldier marching
  38. Occurs randomly and irregularly @ 1 Hz-500 Hz Signals Originate from spinal cord or peripheral nerve lesion causing contrctn of ms Due to involuntary asynchronous contraction of bundles of ms fibers or a whole motor unit Can occur in healthy individual or in diseases Can be seen with naked eye Sound: low pitched dump
  39. Occurs randomly and irregularly @ 1 Hz-500 Hz Signals Originate from spinal cord or peripheral nerve lesion causing contrctn of ms Due to involuntary asynchronous contraction of bundles of ms fibers or a whole motor unit Can occur in healthy individual or in diseases Can be seen with naked eye Sound: low pitched dump
  40. Amplitude: measured from most positive to most negative peak; reflects muscle fiber density close to needle; Rise Time: time lag from initial positive defletion to subsequent negative upward peak: Distance between needle and MU Duration: initial departure from baseline to final return to baseline, Degree of synchrony between muscle fibers Phases: peaks crossing baseline, Normal has 3 peaks, more than 4_ polyphasics
  41. Clear, sharp Sound
  42. Normal Polyphasic seen in : Upto 30 % in Monopolar & 15 % in concentric needle AP of one muscle fiber: represents individual components of phase Myopathic: reflects Regeneration of fibers & increase in fiber density in myopathies Neuropathic: Regeneration of axons in neuropathies
  43. Recruitment: Interference
  44. On voluntary contraction, smaller muscles fibers recruited first then larger: Henneman principle
  45. Myokymia: Due to hyperexcitability of peripheral nerve motor axons
  46. Neuromusculoskeletal assessment: type of lesion, severity Active stage of disease: energy conservations technique Recovery stage: gradual increase in treatment Neuropraxia, Axonotmesis: